Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930022D16Rik |
A |
G |
11: 109,308,855 (GRCm39) |
I74V |
unknown |
Het |
Acss3 |
T |
A |
10: 106,802,890 (GRCm39) |
I452F |
possibly damaging |
Het |
Adam10 |
T |
C |
9: 70,651,173 (GRCm39) |
L66P |
probably damaging |
Het |
Adamts18 |
A |
T |
8: 114,464,245 (GRCm39) |
C738S |
probably damaging |
Het |
Adamts7 |
T |
G |
9: 90,056,593 (GRCm39) |
S221A |
probably damaging |
Het |
Adrm1 |
A |
G |
2: 179,816,648 (GRCm39) |
|
probably benign |
Het |
Aqp1 |
T |
C |
6: 55,313,624 (GRCm39) |
V50A |
possibly damaging |
Het |
Aqp4 |
T |
C |
18: 15,531,183 (GRCm39) |
I193V |
probably benign |
Het |
B130006D01Rik |
A |
T |
11: 95,617,066 (GRCm39) |
|
probably benign |
Het |
Ccdc121rt2 |
A |
G |
5: 112,597,764 (GRCm39) |
S104G |
possibly damaging |
Het |
Ccnl1 |
C |
T |
3: 65,854,131 (GRCm39) |
|
probably benign |
Het |
Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dcdc2a |
T |
A |
13: 25,245,223 (GRCm39) |
L100* |
probably null |
Het |
Eif4g3 |
G |
T |
4: 137,853,769 (GRCm39) |
R618L |
probably benign |
Het |
F5 |
C |
T |
1: 164,036,598 (GRCm39) |
P1920S |
probably benign |
Het |
Fam187b |
T |
A |
7: 30,677,170 (GRCm39) |
N226K |
probably benign |
Het |
Fancc |
C |
A |
13: 63,479,637 (GRCm39) |
|
probably benign |
Het |
Fastk |
G |
T |
5: 24,648,117 (GRCm39) |
P233H |
probably damaging |
Het |
Fbn1 |
A |
C |
2: 125,148,420 (GRCm39) |
D2609E |
probably benign |
Het |
Fes |
G |
A |
7: 80,036,959 (GRCm39) |
R42W |
probably damaging |
Het |
Fmnl2 |
T |
A |
2: 52,993,728 (GRCm39) |
N374K |
possibly damaging |
Het |
Fpgt |
G |
A |
3: 154,792,333 (GRCm39) |
Q565* |
probably null |
Het |
Gckr |
A |
G |
5: 31,465,141 (GRCm39) |
D370G |
probably damaging |
Het |
Ggt6 |
T |
C |
11: 72,328,769 (GRCm39) |
M385T |
probably benign |
Het |
Gm26657 |
C |
A |
4: 56,741,114 (GRCm39) |
H100N |
probably benign |
Het |
Gsg1l |
T |
A |
7: 125,557,721 (GRCm39) |
I136F |
probably damaging |
Het |
Hhip |
C |
T |
8: 80,724,192 (GRCm39) |
R350Q |
probably damaging |
Het |
Ints1 |
C |
T |
5: 139,745,599 (GRCm39) |
S1353N |
probably benign |
Het |
Ints10 |
G |
A |
8: 69,263,271 (GRCm39) |
R394Q |
probably damaging |
Het |
Ints6 |
T |
G |
14: 62,940,678 (GRCm39) |
R557S |
probably damaging |
Het |
Ints9 |
T |
A |
14: 65,269,729 (GRCm39) |
I473N |
possibly damaging |
Het |
Itih4 |
G |
A |
14: 30,623,626 (GRCm39) |
G915R |
probably damaging |
Het |
Kif1a |
C |
A |
1: 92,952,368 (GRCm39) |
A1304S |
possibly damaging |
Het |
Kif21b |
C |
T |
1: 136,075,924 (GRCm39) |
|
probably benign |
Het |
Klk13 |
C |
A |
7: 43,363,284 (GRCm39) |
C10* |
probably null |
Het |
Krtap4-8 |
C |
T |
11: 99,671,321 (GRCm39) |
|
probably benign |
Het |
Lef1 |
T |
C |
3: 130,978,382 (GRCm39) |
S167P |
probably benign |
Het |
Leng8 |
T |
A |
7: 4,147,796 (GRCm39) |
I607N |
probably damaging |
Het |
Lrch4 |
T |
A |
5: 137,637,408 (GRCm39) |
L526* |
probably null |
Het |
Memo1 |
G |
A |
17: 74,565,456 (GRCm39) |
Q36* |
probably null |
Het |
Nod1 |
C |
A |
6: 54,920,741 (GRCm39) |
A526S |
probably damaging |
Het |
Nostrin |
G |
A |
2: 69,014,243 (GRCm39) |
V400M |
possibly damaging |
Het |
Nrip1 |
T |
C |
16: 76,089,920 (GRCm39) |
T546A |
probably benign |
Het |
Nxf1 |
A |
G |
19: 8,740,127 (GRCm39) |
D98G |
probably benign |
Het |
Or13a24 |
A |
G |
7: 140,154,554 (GRCm39) |
M163V |
probably benign |
Het |
Or1l4 |
T |
A |
2: 37,092,094 (GRCm39) |
Y280* |
probably null |
Het |
Or2h2b-ps1 |
A |
T |
17: 37,481,173 (GRCm39) |
V20E |
probably damaging |
Het |
Or2t1 |
A |
G |
14: 14,328,887 (GRCm38) |
M259V |
probably benign |
Het |
Or4c114 |
G |
T |
2: 88,904,656 (GRCm39) |
P260T |
probably benign |
Het |
Or6aa1 |
A |
T |
7: 86,043,718 (GRCm39) |
|
probably null |
Het |
Osgep |
T |
C |
14: 51,155,378 (GRCm39) |
Y60C |
probably damaging |
Het |
P2ry6 |
A |
G |
7: 100,587,511 (GRCm39) |
Y283H |
probably damaging |
Het |
Pcdha7 |
A |
T |
18: 37,108,870 (GRCm39) |
S632C |
possibly damaging |
Het |
Pms1 |
T |
A |
1: 53,234,097 (GRCm39) |
R806S |
possibly damaging |
Het |
Qars1 |
T |
A |
9: 108,386,625 (GRCm39) |
|
probably null |
Het |
Rxfp1 |
T |
C |
3: 79,594,196 (GRCm39) |
N66S |
probably damaging |
Het |
Slc12a5 |
A |
T |
2: 164,815,685 (GRCm39) |
N67I |
probably damaging |
Het |
Slc1a4 |
G |
T |
11: 20,254,348 (GRCm39) |
T506K |
probably damaging |
Het |
Stimate |
C |
A |
14: 30,594,490 (GRCm39) |
|
probably benign |
Het |
Tlr9 |
T |
A |
9: 106,102,173 (GRCm39) |
I488N |
probably damaging |
Het |
Tmem74 |
G |
T |
15: 43,730,554 (GRCm39) |
T163K |
probably damaging |
Het |
Uba2 |
T |
C |
7: 33,854,021 (GRCm39) |
D307G |
probably damaging |
Het |
Uty |
C |
T |
Y: 1,131,134 (GRCm39) |
R924Q |
probably damaging |
Het |
Wdr7 |
C |
T |
18: 63,910,651 (GRCm39) |
T681I |
probably benign |
Het |
Xab2 |
A |
G |
8: 3,668,105 (GRCm39) |
S158P |
probably benign |
Het |
Ythdc1 |
T |
C |
5: 86,970,667 (GRCm39) |
S418P |
probably damaging |
Het |
Zfand4 |
T |
A |
6: 116,305,195 (GRCm39) |
C207* |
probably null |
Het |
Zfp367 |
C |
T |
13: 64,283,238 (GRCm39) |
D305N |
probably damaging |
Het |
Zfp804b |
C |
T |
5: 6,822,584 (GRCm39) |
V160I |
probably benign |
Het |
|
Other mutations in Bbs10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
chalky
|
UTSW |
10 |
111,135,622 (GRCm39) |
missense |
probably damaging |
1.00 |
wampum
|
UTSW |
10 |
111,135,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0097:Bbs10
|
UTSW |
10 |
111,134,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Bbs10
|
UTSW |
10 |
111,135,194 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0189:Bbs10
|
UTSW |
10 |
111,136,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Bbs10
|
UTSW |
10 |
111,135,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Bbs10
|
UTSW |
10 |
111,135,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1319:Bbs10
|
UTSW |
10 |
111,134,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Bbs10
|
UTSW |
10 |
111,135,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R2015:Bbs10
|
UTSW |
10 |
111,136,716 (GRCm39) |
nonsense |
probably null |
|
R2361:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R3716:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R3717:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4407:Bbs10
|
UTSW |
10 |
111,135,720 (GRCm39) |
missense |
probably benign |
0.00 |
R4583:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4607:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4607:Bbs10
|
UTSW |
10 |
111,136,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R4608:Bbs10
|
UTSW |
10 |
111,136,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R4609:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4646:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4647:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4648:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4730:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4822:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R4832:Bbs10
|
UTSW |
10 |
111,136,995 (GRCm39) |
missense |
probably benign |
0.02 |
R5056:Bbs10
|
UTSW |
10 |
111,136,401 (GRCm39) |
missense |
probably benign |
0.00 |
R6285:Bbs10
|
UTSW |
10 |
111,135,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R6604:Bbs10
|
UTSW |
10 |
111,136,965 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7120:Bbs10
|
UTSW |
10 |
111,135,310 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7174:Bbs10
|
UTSW |
10 |
111,136,628 (GRCm39) |
nonsense |
probably null |
|
R7376:Bbs10
|
UTSW |
10 |
111,135,111 (GRCm39) |
missense |
probably benign |
0.08 |
R7701:Bbs10
|
UTSW |
10 |
111,135,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8146:Bbs10
|
UTSW |
10 |
111,136,396 (GRCm39) |
missense |
probably benign |
0.05 |
R8260:Bbs10
|
UTSW |
10 |
111,136,104 (GRCm39) |
nonsense |
probably null |
|
R8832:Bbs10
|
UTSW |
10 |
111,136,266 (GRCm39) |
nonsense |
probably null |
|
R9656:Bbs10
|
UTSW |
10 |
111,135,545 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Bbs10
|
UTSW |
10 |
111,136,985 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Bbs10
|
UTSW |
10 |
111,135,518 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Bbs10
|
UTSW |
10 |
111,134,769 (GRCm39) |
critical splice donor site |
probably null |
|
|